FDA Inspection 854134 — Synteract, Inc.

Synteract, Inc. — FEI 3003515242

The FDA completed an inspection of Synteract, Inc. on November 4, 2013 in Carlsbad, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 4, 2013
Fiscal Year
2014
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Carlsbad, CA (United States)

Additional Details

Sponsor, Contract Research Organization